Canonical Allele Identifier: PA2825919908
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 215355

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Asp379Asn
CA319808
NM_001145853.1:c.1135G>A